ENST00000477226.6:n.853G>C
|
|
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ENST00000683013.1:n.767G>C
|
|
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ENST00000373960.4:c.1379G>C
MANE Select
|
ENSP00000363071.3:p.Ser460Thr
|
|
ENST00000373960.3:c.1379G>C
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ENSP00000363071.3:p.Ser460Thr
|
|
ENST00000483395.1:n.234G>C
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|
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NM_001927.3:c.1379G>C , LRG_380t1:c.1379G>C
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NP_001918.3:p.Ser460Thr
|
|
NM_001927.4:c.1379G>C
MANE Select
|
NP_001918.3:p.Ser460Thr
|
|
NM_001382708.1:c.1376G>C
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NP_001369637.1:p.Ser459Thr
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NM_001382709.1:c.947G>C
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NP_001369638.1:p.Ser316Thr
|
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NM_001382710.1:c.1310G>C
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NP_001369639.1:p.Ser437Thr
|
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NM_001382711.1:c.1358G>C
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NP_001369640.1:p.Ser453Thr
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NM_001382712.1:c.1371+211G>C
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NP_001369641.1:n.1371+211G>C
|
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NM_001382713.1:c.1109G>C
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NP_001369642.1:p.Ser370Thr
|
|